Success in the medical device industry requires not just meeting, but exceeding quality and regulatory standards. Our Product Quality and Compliance Excellence solutions provide an integrated, seamless production program that spans the entire device lifecycle.
Our proven methodologies ensure insight and traceability at every stage in the process, reflecting fewer adverse events and product recalls, significant cost reductions, and safer, more innovative products.
Success in the medical device industry requires not just meeting, but exceeding quality and regulatory standards. Our Product Quality and Compliance Excellence solutions provide an integrated, seamless production program that spans the entire device lifecycle.
Our proven methodologies ensure insight and traceability at every stage in the process, reflecting fewer adverse events and product recalls, significant cost reductions, and safer, more innovative products.
Learn More About Product Quality & Compliance Excellence
Achieve Product Quality and Compliance Excellence with our solutions for quality control and regulatory compliance in the medical device industry. Operate with the most efficient, cost-effective processes possible thanks to our advanced digital lifecycle management technology.
Medical device companies are challenged to maintain controls for quality assurance and regulatory compliance across every phase of the device lifecycle. To do so, systemic approaches are needed to provide transparency, traceability and early-stage error detection. This is especially true as products continue to become more personalized and complex, and the marketplace continues to become more global and competitive. Our Product Quality and Compliance Excellence solutions provide technology-enabled processes to ensure proactive quality assurance, and are combined with strategies to increase efficiency, minimize risk and enhance product innovation.
With our digitalized, integrated platforms, globally diverse companies can identify and resolve quality issues at the earliest possible stage. By embedding and utilizing analytical data throughout the product lifecycle, med-tech organizations can support higher production rates, reduced cost of goods, and more efficient regulatory-mandated control processes. Also, the likelihood of adverse events or product recalls can be dramatically reduced, if not eliminated entirely. The result is the achievement of true product excellence, which in the end means realizing innovative and safer devices, improved patient outcomes, and significant increases in the bottom line.
With Teamcenter, you can reduce the manual effort and cost of managing and tracking any PLM process. From managing change across disciplines to executing a simple design review to coordinating a response to quality issues, you can focus people on the right tasks with the right data to make the right decisions at the right time. When executing changes, you can ensure all stakeholders understand what is changing and how it affects them.
Ensure product quality in production by understanding the impact of dimensional variation before design release.
Design products with improved ergonomics in mind and assess human factors for operations to help plan safer workplaces.
Meet all technical and performance requirements at cost and on schedule. Our quality management solutions for medical devices give you the ability to improve product quality and reduce costs across the entire product lifecycle.
Leverage the Internet of Things to achieve agility, speed, and compliance at your medical device or pharmaceutical organization. Our solutions are equipping med-tech organizations with the transparency and advanced analytic tools required to gain a competitive edge using big data.
Our manufacturing execution management solutions are a highly sophisticated, scalable, digital suite that delivers multiple capabilities and allows your med-tech organization to combine production efficiency with quality and visibility, as well as production optimization.
Our environmental compliance management solutions for the medical device industry serve as an effective and rapid response to the global quest to protect our planet and its inhabitants. Our systems support sustainability at every phase in the product lifecycle which enable med-tech companies to achieve success on many levels.
高度に記述的な技術文書は、それによって製造およびサービスチームの生産性が向上する場合は特に、非常に有益なことがあります。RapidAuthor for Teamcenterを使用すると、エンジニアリング設計データのコンテンツを技術ドキュメントで直接再利用できるので、その投資が無駄になりません。CADおよびPLM XMLのコンテンツは、テキストと2D/3Dグラフィックおよびアニメーションに直接変換されるため、製品の仕組みと、製品の製造とサービスを行うのに必要な決定事項をよりよく理解できます。
Manage product requirements with our systematic and repeatable solution for building-in the voice of the customer, enabling medical device companies to easily capture, securely manage, accurately verify, and reliably maintain requirements information across the entire device lifecycle.
With Teamcenter, you can reduce the manual effort and cost of managing and tracking any PLM process. From managing change across disciplines to executing a simple design review to coordinating a response to quality issues, you can focus people on the right tasks with the right data to make the right decisions at the right time. When executing changes, you can ensure all stakeholders understand what is changing and how it affects them.
Leverage the Internet of Things to achieve agility, speed, and compliance at your medical device or pharmaceutical organization. Our solutions are equipping med-tech organizations with the transparency and advanced analytic tools required to gain a competitive edge using big data.
Our manufacturing execution management solutions are a highly sophisticated, scalable, digital suite that delivers multiple capabilities and allows your med-tech organization to combine production efficiency with quality and visibility, as well as production optimization.
Our environmental compliance management solutions for the medical device industry serve as an effective and rapid response to the global quest to protect our planet and its inhabitants. Our systems support sustainability at every phase in the product lifecycle which enable med-tech companies to achieve success on many levels.
Manage product requirements with our systematic and repeatable solution for building-in the voice of the customer, enabling medical device companies to easily capture, securely manage, accurately verify, and reliably maintain requirements information across the entire device lifecycle.
Siemens and PRISYM ID discuss the key to optimized labeling
Explore our solutions to ensure product quality, compliance, and profitability.
Risk management and compliance are key for medical device manufacturers.
医療機器の製品管理をエンドツーエンドで行うシーメンスの多分野ソリューション
